C M Moorman1, J S Elston, P Matthews. Show Affiliations » 1. Oxford Eye Hospital, England.
Abstract
Entities: Disease Mutation
Mesh: See more » ChildDNA, Mitochondrial/geneticsHumansMaleMutationOptic Atrophies, Hereditary/complicationsOptic Atrophies, Hereditary/geneticsVision, Low/etiologyVision, Low/genetics
Substances: See more » DNA, Mitochondrial
Year: 1993 PMID: 8474822
Source DB: PubMed Journal: Pediatrics ISSN: 0031-4005 Impact factor: 7.124